CAR T-cell therapy for B-cell lymphomas: clinical trial results of available products

被引:173
作者
Chavez, Julio C. [1 ]
Bachmeier, Christina [2 ]
Kharfan-Dabaja, Mohamed A. [3 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, 12902 Magnolia Dr, Tampa, FL 33612 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Blood & Marrow Transplantat, Tampa, FL 33612 USA
[3] Mayo Clin, Div Hematol Oncol, Jacksonville, FL 32224 USA
关键词
B-cell lymphoma; chimeric antigen receptor; cytokine-release syndrome; immunotherapy; refractory; CHIMERIC-ANTIGEN-RECEPTOR; RITUXIMAB PLUS CYCLOPHOSPHAMIDE; BONE-MARROW-TRANSPLANTATION; DETUDES DES LYMPHOMES; NON-HODGKIN-LYMPHOMA; FOLLICULAR LYMPHOMA; ADOPTIVE IMMUNOTHERAPY; ALLOGENEIC TRANSPLANTATION; CONDITIONING REGIMENS; PHASE-2; MULTICENTER;
D O I
10.1177/2040620719841581
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adoptive cellular immunotherapy with chimeric antigen receptor (CAR) T cell has changed the treatment landscape of B-cell non-Hodgkin's lymphoma (NHL), especially for aggressive B-cell lymphomas. Single-center and multicenter clinical trials with anti-CD19 CAR T-cell therapy have shown great activity and long-term remissions in poor-risk diffuse large B-cell lymphoma (DLBCL) when no other effective treatment options are available. Two CAR T-cell products [axicabtagene ciloleucel (axi-cel) and tisagenlecleucel] have obtained US Food and Drug Administration approval for the treatment of refractory DLBCL after two lines of therapy. A third product, liso-cel, is currently being evaluated in clinical trials and preliminary results appear very promising. CAR T-cell-related toxicity with cytokine-release syndrome and neurotoxicity remain important potential complications of this therapy. Here, we review the s biology, structure, clinical trial results and toxicity of two commercially approved CAR T-cell products and others currently being studied in multicenter clinical trials in B-cell NHLs.
引用
收藏
页码:1 / 20
页数:20
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